713 results • Page 9 of 12
Hi folks, I am having a trouble with dba.count function in diffbind. It fails with warnings but without any specific information. Please see below: > obj <- dba(sampleSheet='analysis...nbsp;methods   \[9\] base      other attached packages:  \[1\] DiffBind\_2.4.8             S…
in diffbind when perform this: tamoxifen <- dba.contrast(tamoxifen,+ reorderMeta=list(Condition="Responsive")) then at the results
updated 7 weeks ago • Jeffcgen2000
that we can use for the analysis of differential binding ? (I do not have access to the packages DiffBind or derfinder) ; much thanks, Bogdan
updated 2.1 years ago • Bogdan
I am trying out different DiffBind normalization methods for my ATAC-seq dataset in order to select the most suitable one. However, it looks like no...I am trying out different DiffBind normalization methods for my ATAC-seq dataset in order to select the most suitable one. However, it looks like no matter
updated 2.6 years ago • bers.anthrope
Hi, I am using dba.plotvenn to plot overlapped binding sites between three groups. I have created a three-way Venn diagram, but I do not like how it looks. As the picture shows, numbers "16782" and "5632" are not where they are supposed to be. Also, group #2 is on the line, which needs to be shifted to the right a bit. I am looking everywhere, but the answer is nowhere. Please help …
updated 4.1 years ago • jiekwo1
Hi! I am trying to run Diffbind with DESeq2 on my Cut&Run dataset. I have tried multiple normalization methods in dba.count() and dba.normalize
I would like to compare two conditions with each two ChIP-seq (H3K27me3) samples. I searched for tools for differential binding and found that many including diffbind and csaw compares two conditions with read counts from pull down library only, not using input/control library/read...seq (H3K27me3) samples. I searched for tools for differential binding and found that many including diffbind and c…
updated 6.4 years ago • bioinfo
Dear all, I have bed files with ChIP-seq data, with sequence (chromosome) names like this: chr1, chr10, chr11, chr12, chr13, chr13\_random, chr14, . . ., chrX I  import the bed file data into a DiffBind DBA object using the command > dbaObj <-  dba(sampleSheet = "samples.csv") The problem is that the chromosome names...chr11, chr12, chr13, chr13\_random, chr14…
updated 10.0 years ago • Georg Otto
function, and subsequently dba.analyze(). I basically followed the steps on page 45 of the Diffbind documentation. https://bioconductor.org/packages/release/bioc/vignettes/DiffBind/inst/doc/DiffBind.pdf However...or scripts of runnning successful offset and loess normalization? Thank you! ```r library(DiffBind) library(edgeR) library(tidyverse) library(dplyr) samples <…
updated 7 months ago • Henry
Hello! I am currently using DiffBind 3.6.1 and encountering the following error when attempting to analyze my data: ```r > dba <- dba.contrast(dba, design
updated 2.4 years ago • millerh1
Hello there, I am just started playing with ChIPQC and DiffBind but I am failing miserably at just loading the sample data.&nbsp; I have downloaded the DiffBind Package data from...your website (https://www.dropbox.com/s/gfc49wul2bv5nz6/DiffBind\_vignette\_data.tar.gz) My script looks like: <pre> # load libraries library(ChIPQC) library(DiffBind) # read in files
updated 6.3 years ago • avp25
files i.e `125`. P.S: from github the error stems from this section : https://github.com/aeron15/DiffBind/blob/master/R/counts.R#L579 but I'm not familiar with what those lines mean. R version 4.1.0 (2021-05-18) Platform: x86_64
updated 3.5 years ago • Alexandre
compare them to identify enriched regions. In the case, can I use default DESeq2 pipeline similar as DiffBind ? Or Do I need to use one-sided test for enriched regions ? As I understand, if I want to check both enriched or depleted
updated 4.7 years ago • bioinfo
Hello, I've been using DiffBind for my analyses and it's working great, apart from a specific problem I encountered with the output: Sometimes it...Hello, I've been using DiffBind for my analyses and it's working great, apart from a specific problem I encountered with the output: Sometimes it will
updated 2.9 years ago • mhw46
<div class="preformatted">Hi Alejandra- First, can you check the versions you are using by sending the output of sessionInfo()? The color bars were added to DiffBind at some point and are not present in all versions. You need version 1.4.0 or later, which corresponds to Bioconductor 2.11 (R 2.15). Next, check the help page for dba.plotHeatmap: &gt; ?dba.plotHeatmap All of the heatma…
updated 11.6 years ago • Rory Stark
Dear&nbsp;Rory Stark, Thanks for DiffBind package for analyzing ChIP-seq dataset that has multiple replicates. I encountered two issues when trying to add
updated 6.1 years ago • yuhongning2013
Hi I had a question about the following example in the diffbind tutorial: # Plot effect of a range of filter values and then apply filter data(tamoxifen_counts) rate.max &lt;- dba.count
updated 5.1 years ago • rbronste
Conc**(which is showed in final dba.report) and **score**. Let's make a example ``` library(DiffBind) library(BiocParallel) library(dplyr) tamoxifen &lt;- dba(sampleSheet="tamoxifen.csv") tamoxifen &lt;- dba.count(tamoxifen
updated 3.8 years ago • shangguandong1996
Hi, I'm trying to run DiffBind `3.4.11` on R `4.1.2` on some bed files created using bedtools merge, so they look like: ```r 1 1875658 1934008 EdU_HU_HME1_sgMSL1_R1_peak_54
updated 2.0 years ago • Pablo
Hi there, Thank you for developing DiffBind package! I am running through the vignette. It is really helpful. I see the codes using `dbs.all` in Section 7.5. But I...Hi there, Thank you for developing DiffBind package! I am running through the vignette. It is really helpful. I see the codes using `dbs.all` in Section 7.5. But I do
updated 2.8 years ago • Mark
Enter the body of text here Code should be placed in three backticks as shown below ```r # include your problematic code here with any corresponding output # please also include the results of running the following in an R session sessionInfo( ) cell <- dba(sampleSheet = "/home/cytolab/extdata/cell lines data.csv") 1 cal27 ko1 H3K36me2 Treated full media 1 bed Error in if (file.info(pe…
updated 16 months ago • ANAMIKA
I have a very simple question: how can I check my version of an installed package - in this case DiffBind? I know a simple `-v` in Unix achieves this, but I can't seem to figure it out in R. Part of the reason I need to know is because
updated 3.9 years ago • bertb
Hi All, I have Chip-Seq data for histone marks (H3K27me3, H3K27ac, H3K4me1 and H3K4me3) for 2 different cancer subtypes which differ in their aggressiveness. I am interested to see if there is any association between the tumor aggressiveness and H3K27me3 loss. I have used Diffbind to call differential binding sites between different subtypes for each antibody. I read it somewhere that the H3K…
updated 5.2 years ago • researcher
Hello Everyone, &nbsp; Let me start by saying I've read all posts that are similar to my question and the insights are tremendous! However, as I've been doing bioinformatics for a little over a year now, I'm still a newbie in all possible respects, and I just want a clarification. &nbsp; So here's the gist. I have replicates of three conditions (each with its own Input). What I first …
updated 6.0 years ago • Yonatan Amzaleg
sequence coverage difference between replicates and among samples? I am using DESeq2 and edgeR in DiffBind to compare ATAC-seq samples with different sequencing coverage among samples, from 77 to 25 million reads, and up
updated 2.1 years ago • cesar.arenasmena
Hello All, I have 300 chIP peaksets. I am trying to count and analyze them using DiffBind. However when I am running the code, I get the following error. Will appreciate any suggestion to fix it. Many thanks
dds)) &gt; 10, ]</pre> I obtain the count matrices from ChIP-seq and ATAC-seq experiments through DiffBind and then use DESeq2 for the differential binding analysis. I guess its a bit of an arbitrary cutoff, but wondering
div class="preformatted">Hi I have been trying to use DiffBind to analyze our Chip-seq data and have been running into some errors repeatedly. I first created a samplesheet.csv...each and the peaks were called using MACS v2. The peak caller generated .bed files which was used in DiffBind. I defined the working directory in R first. I then read the sample sheet in : &gt; H3K4.B73=dba(s…
updated 11.2 years ago • Anitha Sundararajan
please help me, I will be very grateful.&nbsp; I am trying to do the dba.count command out of the DiffBind package in R. Creating the dba object works fine for me, but when I wanted to do the counting, this error occurs: &gt; counts.runx1...nbsp; &nbsp; datasets &nbsp;methods &nbsp; base &nbsp; &nbsp;&nbsp; other attached packages: \[1\] DiffBind\_1.8.5 &…
updated 7.6 years ago • jorrenkuster
Hello, I am running DiffBind analysis on a ChIP-Seq dataset, comparing Control versus Treatment and using Factor(Donor IDs) as a blocking factor...of estimateDispersionsFit within the DESeq2 model. How do I implement this change through DiffBind? *** ####My code: dat.bind &lt;- dba.contrast(dat.bind, group1=dat.bind$masks$cond1, group2=dat.bind$masks$cond0, name1=cond1...…
updated 5.9 years ago • avantika6194
I am attempting to perform differential peak analysis from ATAC-seq data using DiffBind package and am running into problems with the dba.count function. I have 2 conditions (rapid vs slow) with 3 samples
updated 5.3 years ago • chadnewton
analyzing large data set and to speed up things I am going to use cluster.&nbsp; I am working with DiffBind packadge and I will create a single GRanges object that will be used for dba.counts function to create few smaller
updated 6.5 years ago • Lauma R
the same problem?</span> &nbsp; &nbsp; <span style="line-height:1.6">I have&nbsp;</span>&nbsp;DiffBind\_1.10.2&nbsp;version and&nbsp;R version 3.1.0 &nbsp; <span style="line-height:1.6">Thanks in advance. </span> &nbsp; <span style
updated 10.1 years ago • sergio.espeso-gil
Hi Rory, &nbsp; &nbsp; I am trying diffBind on my ATAC-seq data. And I have difficulties on using db.count() function. I got error message as below. Error in pv.counts
updated 9.6 years ago • yijing.su
Hello, I have a question about figure 13 in the Diffbind manual. &nbsp;according to this part (page4,&nbsp;&gt; tamoxifen &lt;- dba(sampleSheet="tamoxifen.csv") :&nbsp; 3 MCF71 MCF7...Hello, I have a question about figure 13 in the Diffbind manual. &nbsp;according to this part (page4,&nbsp;&gt; tamoxifen &lt;- dba(sampleSheet="tamoxifen.csv") :&nbsp; 3 …
updated 7.5 years ago • mforoo1
with 12 bed files, i get this from str(dba): ```$ totalMerged: int 42967 $ called : num [1:42967, 1:12] 0 1 1 1 0 0 1 1 1 1 ... $ merged : num [1:42967, 1:3] 1 1 1 1 1 1 1 1 1 1 ... ``` with 11 bed files, i get this from str(dba): ```$ totalMerged: int 42967 $ called : num [1:3477, 1:11] 0 0 0 0 0 0 0 0 0 0 ... $ merged : num [1:42967, 1:3] 1 1 1 1 1 1 1 1 1 1 ... ``` wha…
updated 2.3 years ago • Nicole
I have 10 "summit" bed files from macs2 peak-calling, with 5 factors with 2 replicates each. I added them all one-by-one to a dba object "dbObj" that looks like this: 10 Samples, 3202 sites in matrix (234027 total): ID Factor Replicate Caller Intervals 1 CTR-1 ctr 1 bed 29940 2 CTR-2 ctr 2…
updated 4.7 years ago • hkitano
Trying to set up a contrast based on some masks and having some problems. The __dba.count__ looks as follows:  12 Samples, 1054182 sites in matrix (2657422 total):      ID Tissue Factor Condition Treatment Replicate Caller Intervals
1  MBV1  BN1     DR      MALE   VEHICLE         1 narrow    500000

2  MBV2  BN1     DR      MALE   VEHICLE         2 narrow    281265

3…
updated 7.3 years ago • rbronste
When you retrieve the differentially bound sites with `` dba.report() ``, there is a "Conc" column that shows the mean read concentration over all the samples (log2 normalized ChIP read counts with control read counts subtracted). Is there a way to calculate those numbers for arbitrary regions (not just differentially bound)?
updated 9.4 years ago • igor
Trying to generate replicate masks for the dba.count function from a .csv where I list 3 replicates under DBA\_CONDITION. Want to do dba.counts with minMembers = 3 to include only those that are in all 3 of each replicate group for the binding matrix. Any clues on how to do this? Thanks.
updated 7.3 years ago • rbronste
Hi ! Hi I want to draw a venn diagram of the peaks shared across four Tissues in my data set, but I'm not able to correctly select the set of peaks or create a contrast that achieves this. The idea is to get four way vennDiagram with the four Tissues. I have tried different things > Example.data <- dba(sampleSheet=Example.table, minOverlap=1) > Example.data.counts <- dba.count…
updated 8.8 years ago • medinaale
Hi Rory, I had been previously, not marking duplicates or removing them in my ChIP-Seq datasets, and instead setting the dba.count bRemoveDuplicates to TRUE. Firstly, how adverse is this strategy when determining differential peaks? And secondly, how does setting bUseSummarizeOverlaps to TRUEcompare to bRemoveDuplicates? Thanks,
Hi all, so I got the following from ATAC-seq samples > ATAC_seq_Goett_peaks 11 Samples, 47306 sites in matrix: ID Tissue Factor Replicate Caller Intervals FRiP 1 Cell1px8old epithelial Cell1 1 counts 47306 0.19 2 Cell1_3rd epithelial Cell1 2 counts 47306 0.18 3 Cell1px11new epithelial Cell1 …
updated 5.2 years ago • theodore.georgomanolis
I tried running the dba.count function and got the following error message? The bam files seem to be fine. --- > chip_seq=chip_seq(tamoxifen,summit=250)
Error: Error processing one or more read files. Check warnings().
In addition: There were 28 warnings (use warnings() to see them)
> warnings()
Warning messages:
1: 
2: 
3: 
4: 
5: 
6: 
7: 
8…
updated 6.6 years ago • hhhcce
Hi, I just wanted to get some clarification on MA plots and exactly what they represent. Including one I made of my diff peak data. I am wondering what the darker blue area is close to the origin as well as further down the log concentration and exactly what it represents in comparison with the lighter blue? Also maybe in this context what is the log concentration representing? Thanks for the cl…
updated 7.8 years ago • rbronste
Hello, I am trying to calculate the FRiP score through `` dba.count() `` method as following, and I've been continuously getting this warning: > compareCount <- dba.count(compare, bParallel=FALSE) Sample: trimmed_DKO_R1.fastq.gz.sam.sort.clean.bam125 Sample: trimmed_DKO_R2.fastq.gz.sam.sort.clean.bam125 Sample: trimmed_HCT116_R1.fastq.gz.sam.sort.…
updated 6.8 years ago • ghosos
Hi, bam files for example execution are missing through installation. How can I find these test bams? Thanks, Kübra
updated 7.6 years ago • kbrnrc
div class="preformatted"> I have been trying to use DiffBind to analyze our Chip-seq data and have been running into some errors repeatedly. I first created a samplesheet.csv...each and the peaks were called using MACS v2. The peak caller generated .bed files which was used in DiffBind. I defined the working directory in R first. I then read the sample sheet in : &gt; H3K4.B73=dba(sampleS…
updated 11.2 years ago • Guest User
Hi all, I have a questions about bulk ATAc seq that could not find out myself and also on Biostar. I use Diffbind to get the table below (differential accessibility regions) and then use ChipPeakAnno to annotate the peaks in the...I have a questions about bulk ATAc seq that could not find out myself and also on Biostar. I use Diffbind to get the table below (differential accessibility regions) a…
updated 14 months ago • Chris
&nbsp; &nbsp; Having trouble to get the ChIPQC to work properly. My ultimate goal is to have the html report generated using&nbsp;ChIPQCreport(). I read in the bam files through dba function in the DiffBind package. All went well and I was able to run all DiffBind functions. Using the same sample sheet and dba object does not work with ChIPQC.&nbsp; I tried read in sample shee…
updated 6.2 years ago • molly_the_minotaur
the problem, I have tried to use a csv table and also a single sample and even using dba object from DiffBind , but I have always this error message: &nbsp; \[bam\_index\_load\] fail to load BAM index. Error: 16 errors; first error: &nbsp
updated 9.9 years ago • sergio.espeso-gil
do I need to create something else? Right now this is my R script: ``` library(ChIPQC) library(DiffBind) library(tidyverse) sampleSheet &lt;- read.csv("meta/peaks.xls") db &lt;- dba(sampleSheet =sampleSheet) ``` When I look at the
updated 2.0 years ago • stacy.genovese
Hi, I have a error from dba.count DBdata <- dba.count(DBdata,summits = TRUE) Computing summits... Error in pv$called[, mask] : subscript out of bounds Can you let me know how to fix this? Thank you!
updated 3.2 years ago • Yoon Hee
Dear friends, While I was using the latest release (3.13), I have met a few problems which need your help. 1. I have repeated the whole process following the vignettes using the built in data sets, but my final results (I got 246 significantly differentially binding sites, see the attached file) are different from numbers (249) provided by the vignettes . 2. Those 246 sites w…
updated 3.5 years ago • skyyks123
Hello,  am wondering if it is possible to call the function dba.contrast without the controls files (i do not have them). I have created a DBA odject as follow: mESC <- dba.peakset(NULL, bamReads = "/home/tandrean/Desktop/mESC/1.sorted.bam", bamControl = NULL,                       peaks="/home/tandrean/Desktop/mESC/1.test\_peaks…
updated 7.8 years ago • fusion.slope
hi,I run the code successfully: ```r yap <- dba.count(yap) yap <- dba.contrast(yap,categories=DBA_CONDITION,minMembers=2) yap 4 Samples, 31676 sites in matrix: ID Condition Treatment Replicate Caller Intervals FRiP 1 IP1 IP IP 1 counts 31676 0.53 2 IP2 IP IP 2 counts 31676 0.56 3 IgG1 IgG IgG 1 counts…
updated 3.6 years ago • 浩然
Hi, When I run dba.counts, it showed an error below (fig1): Error in pv.counts(DBA, peaks = peaks, minOverlap = minOverlap, defaultScore = score,  : Some read files could not be accessed. See warnings for details. In addition: Warning message: not accessible Is it because that I don’t have bamControl for 6 ATAC-Seq samples (fig2)? How can I overcome this issue? Thank you so much. Best, …
updated 8.3 years ago • Gary
shared' peaks (which shared within the two &gt;conditions)? &gt;Is there a way that DiffBind can report on all the condition- exclusive &gt;peaks (ones that are deposited only in one condition but have zero &gt...containing the vignette data &gt; &gt;Hi Gord, &gt; &gt;Thanks for you reply and for the wonderful DiffBind tool! &gt; &gt;I've got the link for t…
updated 10.8 years ago • Rory Stark
not exist, also good. ``` Result: Nope, no chr21 in any of the 8 peak files ## What does DiffBind see? ```r &gt; sample = dba(sampleSheet=read.csv('sample_table.csv'), \ peakFormat='bed', scoreCol=5, bLowerScoreBetter=FALSE
updated 2.6 years ago • Mehmet
Hello, I hope you are doing well and are safe. I wanted to reach out since I have been having issues with loading my broadPeaks and/or the .xls outputs from MACS2 into DiffBind. Would appreciate any help you can provide, thank you! My thinking is there might be something wrong with the way I am...since I have been having issues with loading my broadPeaks and/or the .xls outputs from MACS2 into Di…
updated 19 months ago • Mark
713 results • Page 9 of 12
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